EP1056487A1 - Bioabbaubare polymere mit formgedächtnis - Google Patents

Bioabbaubare polymere mit formgedächtnis

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Publication number
EP1056487A1
EP1056487A1 EP99908402A EP99908402A EP1056487A1 EP 1056487 A1 EP1056487 A1 EP 1056487A1 EP 99908402 A EP99908402 A EP 99908402A EP 99908402 A EP99908402 A EP 99908402A EP 1056487 A1 EP1056487 A1 EP 1056487A1
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Prior art keywords
polymer
composition
segment
shape memory
polymers
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EP99908402A
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English (en)
French (fr)
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EP1056487B1 (de
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Robert S. Langer
Andreas Lendlein
Annette Schmidt
Hans Grablowitz
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Massachusetts Institute of Technology
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Massachusetts Institute of Technology
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
    • A61L31/14—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
    • A61L31/148—Materials at least partially resorbable by the body
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/14—Macromolecular materials
    • A61L27/18—Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
    • A61L27/58—Materials at least partially resorbable by the body
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
    • A61L29/14—Materials characterised by their function or physical properties, e.g. lubricating compositions
    • A61L29/148—Materials at least partially resorbable by the body
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods
    • A61B2017/00831—Material properties
    • A61B2017/00867—Material properties shape memory effect
    • A61B2017/00871—Material properties shape memory effect polymeric
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2400/00—Materials characterised by their function or physical properties
    • A61L2400/16—Materials with shape-memory or superelastic properties

Definitions

  • This application is generally in the area of shape memory polymers, and more particularly to biodegradable shape memory polymers.
  • Shape memory is the ability of a material to remember its original shape, either after mechanical deformation ( Figure 1), which is a one-way effect, or by cooling and heating ( Figure 2), which is a two-way effect. This phenomenon is based on a structural phase transformation.
  • the first materials known to have these properties were shape memory metal alloys (SMAs), including TiNi (Nitinol), CuZnAl, and FeNiAl alloys.
  • SMAs shape memory metal alloys
  • TiNi Ni
  • CuZnAl CuZnAl
  • FeNiAl alloys The structure phase transformation of these materials is known as a martensitic transformation.
  • SMAs shape memory metal alloys
  • These materials have been proposed for various uses, including vascular stents, medical guidewires, orthodontic wires, vibration dampers, pipe couplings, electrical connectors, thermostats, actuators, eyeglass frames, and brassiere underwires. These materials have not yet been widely used, in part because they are relatively expensive.
  • SMPs Shape memory polymers
  • SMAs Shape memory polymers
  • the hard segment is typically crystalline, with a defined melting point
  • the soft segment is typically amorphous, with a defined glass transition temperature.
  • the hard segment is amorphous and has a glass transition temperature rather than a melting point.
  • the soft segment is crystalline and has a melting point rather than a glass transition temperature. The melting point or glass transition temperature of the soft segment is substantially less than the melting point or glass transition temperature of the hard segment.
  • the material When the SMP is heated above the melting point or glass transition temperature of the hard segment, the material can be shaped.
  • This (original) shape can be memorized by cooling the SMP below the melting point or glass transition temperature of the hard segment.
  • a new (temporary) shape is fixed.
  • the original shape is recovered by heating the material above the melting point or glass transition temperature of the soft segment but below the melting point or glass transition temperature of the hard segment.
  • the material is deformed at a temperature lower than the melting point or glass transition temperature of the soft segment, resulting in stress and strain being absorbed by the soft segment.
  • the thermal shape memory effect properties that describe the shape memory capabilities of a material are the shape recovery of the original shape and the shape fixity of the temporary shape.
  • SMPs other than the ability to memorize shape are significantly altered in response to external changes in temperature and stress, particularly at the melting point or glass transition temperature of the soft segment.
  • These properties include the elastic modulus, hardness, flexibility, vapor permeability, damping, index of refraction, and dielectric constant.
  • the elastic modulus (the ratio of the stress in a body to the corresponding strain) of an SMP can change by a factor of up to 200 when heated above the melting point or glass transition temperature of the soft segment.
  • the hardness of the material changes dramatically when the soft segment is at or above its melting point or glass transition temperature.
  • the damping ability can be up to five times higher than a conventional rubber product. The material can readily recover to its original molded shape following numerous thermal cycles, and can be heated above the melting point of the hard segment and reshaped and cooled to fix a new original shape.
  • shape memory polymers generally are segmented polyurethanes and have hard segments that include aromatic moieties.
  • U.S. Patent No. 5, 145,935 to Hayashi discloses a shape memory polyurethane elastomer molded article formed from a polyurethane elastomer polymerized from of a difunctional diiiosicyanate, a difunctional polyol, and a difunctional chain extender.
  • polymers used to prepare hard and soft segments of known SMPs include various polyethers, polyacrylates, polyamides, polysiloxanes, polyurethanes, polyether amides, polyurethane/ureas, polyether esters, and urethane/butadiene copolymers. See, for example, U.S. Patent No. 5,506,300 to Ward et al.; U.S. Patent No. 5, 145,935 to Hayashi; U.S. Patent No. 5,665,822 to Bitler et al.; and Gorden, "Applications of Shape Memory Polyurethanes," Proceedings of the First International Conference on Shape Memory and Superelastic Technologies, SMST International Committee, pp. 115-19 (1994).
  • biodegradable shape memory polymers It is therefore an object of the present invention to provide biodegradable shape memory polymers. It is still a further object of the present invention to provide shape memory polymers with physical and chemical properties and chemical structures that are different than those in conventional shape memory polymers.
  • Biodegradable shape memory polymer compositions include one or more hard segments and one or more soft segments, wherein the compositions are biocompatible and at least one of the segments is biodegradable or at least one of the segments is linked to another segment via a biodegradable linkage.
  • the melting point or glass transition temperature (hereinafter, the Ttrans) of the hard segment is at least 10 °C, and preferably 20 °C, higher than the Ttrans of the soft segment.
  • the Trans of the hard segment is preferably between -30 and 270 °C, and more preferably between 30 and 150 °C.
  • the ratio by weight of the hard segment: soft segments is between about 5:95 and 95:5, preferably between 20:80 and 80:20.
  • the shape memory polymers contain at least one physical crosslink (physical interaction of the hard segment) or contain covalent crosslinks instead of a hard segment.
  • the shape memory polymers can also be interpenetrating networks or a semi- interpenetrating networks.
  • hard and soft segments may undergo solid to solid state transitions, and can undergo ionic interactions involving polyelectrolyte segments or supramolecular effects based on highly organized hydrogen bonds.
  • biodegradable polymers include polyhydroxy acids, polyalkanoates, polyanhydrides, polyphosphazenes, polyetheresters, polyesteramides, polyesters, and polyorthoesters.
  • Exemplary biodegradable linkages include ester, amide, anhydride, carbonate, and orthoester linkages.
  • Articles of manufacture can be prepared from the shape memory polymer compositions, for example, by injection molding, blowing, extrusion, and laser ablation.
  • the object can be formed at a temperature above the Tra n s of the hard segment, and cooled to a temperature below the Ttrans of the soft segment. If the object subsequently is formed into a second shape, the object can be returned to its original shape by heating the object above the T tr ans of the soft segment and below the T ran s of the hard segment.
  • Thermoset polymers can be prepared by pre-shaping macromonomers, for example, by extrusion, and fix-ing the original shape at a temperature above the T ⁇ ans of the thermoset polymer, for example, by photocuring reactive groups on the macromonomer.
  • Figure 2 is an illustration of the two-way (thermal) shape memory effect.
  • Figure 3 is an illustration of combinations of suitable classes of thermoplastic materials.
  • Figure 4 is a diagram of a reaction sequence for the synthesis of a preferred photocrosslinker.
  • Figure 5 is an illustration of a photoinduced shape memory effect.
  • Figure 6 is an illustration of the mechanism of the thermal shape memory effect for a multiblock copolymer.
  • Figure 7 is a graph showing stress versus elongation for a multi-block copolymer shape memory polymer.
  • Figure 8 is a graph showing the melting temperature of diols, dimethacrylates, and thermosets of poly( ⁇ -caprolactone) as a function of the molar mass weight M consult of the macromonomers.
  • Biodegradable shape memory polymer compositions are described. Definitions
  • biodegradable refers to materials that are bioresorbable and/or degrade and/or break down by mechanical degradation upon interaction with a physiological environment into components that are metabolizable or excretable, over a period of time from minutes to three years, preferably less than one year, while maintaining the requisite structural integrity.
  • degrade refers to cleavage of the polymer chain, such that the molecular weight stays approximately constant at the oligomer level and particles of polymer remain following degradation.
  • completely degrade refers to cleavage of the polymer at the molecular level such that there is essentially complete mass loss.
  • degrade as used herein includes “completely degrade” unless otherwise indicated.
  • a polymer is a shape memory polymer if the original shape of the polymer is recovered by heating it above a shape recovering temperature (defined as the T trans of a soft segment) even if the original molded shape of the polymer is destroyed mechanically at a lower temperature than the shape recovering temperature, or if the memorized shape is recoverable by application of another stimulus.
  • a shape recovering temperature defined as the T trans of a soft segment
  • segment refers to a block or sequence of polymer forming part of the shape memory polymer.
  • hard segment and soft segment are relative terms, relating to the Ttraa of the segments.
  • the hard segment(s) has a higher Ttrans than the soft segment(s).
  • the shape memory polymers can include at least one hard segment and at least one soft segment, or can include at least one kind of soft segment wherein at least one kind of the soft segments are crosslinked, without the presence of a hard segment.
  • the hard segments can be linear oligomers or polymers, and can be cyclic compounds, such as crown ethers, cyclic di-, tri-, or oligopetides, and cyclic oligo(ester amides).
  • the physical interaction between hard segments can be based on charge transfer complexes, hydrogen bonds, or other interactions, since some segments have melting temperatures that are higher than the degradation temperature. In these cases, there is no melting or glass transition temperature for the segment.
  • a non-thermal mechanism such as a solvent, is required to change the segment bonding.
  • the ratio by weight of the hard segment: soft segments is between about 5:95 and 95:5, preferably between 20:80 and 80:20.
  • Shape Memory Polymeric Compositions Thermoplastic shape memory materials are shaped/molded to a desired shape above the Tt ran s of the hard segment(s) and cooled down to a temperature below the shape recovering temperature, where the polymer may undergo mechanical deformation and strains are generated in the polymer.
  • thermoset shape memory materials are shaped/molded to a desired shape before the macromonomers used to form the thermoset polymers are polymerized. After the shape has been fixed, the macromonomers are polymerized.
  • the polymer compositions are preferably compressible by at least one percent or expandable by at least five one of the original thickness at a temperature below the shape recovering temperature, with the deformation being fixed by application of a stimulus such as heat, light, ultrasound, magnetic fields or electric fields.
  • a stimulus such as heat, light, ultrasound, magnetic fields or electric fields.
  • the materials show a ratio of recovery of 98% (compare to experimental examples).
  • SM polymer can undergo solid state to solid state transitions (e.g. change in morphology). Solid state to solid state transitions are well known to those of skill in the art, e.g. in poly(styrene-b/oc&-butadiene).
  • the changes in shape can be two dimensional. If the objects are essentially two dimensional objects, such as fibers, then the changes in shape can be one dimensional, such as along the length.
  • the thermal and electrical conductivity of the materials can also change in response to changes in temperature.
  • the moisture permeability of the compositions can be varied, especially when the polymer is formed into a thin film (i.e., less than about 10 ⁇ m).
  • the resulting materials have low moisture permeability at temperatures below room temperature and high moisture permeability at temperatures above room temperature.
  • Stimuli other than temperature can be used to induce shape changes.
  • shape changes can be elicited by exposure to light activation or an agent such as an ion which alters the interpolymer bonds.
  • the segments preferably are oligomers.
  • oligomer refers to a linear chain molecule having a molecular weight up to 15,000 Da.
  • the polymers are selected based on the desired glass transition temperature(s) (if at least one segment is amorphous) or the melting point(s) (if at least one segment is crystalline), which in turn is based on the desired applications, taking into consideration the environment of use.
  • the number average molecular weight of the polymer block is greater than 400, and is preferably in the range of between 500 and 15,000.
  • the transition temperature at which the polymer abruptly becomes soft and deforms can be controlled by changing the monomer composition and the kind of monomer, which enables one to adjust the shape memory effect at a desired temperature.
  • the thermal properties of the polymers can be detected, for example, by dynamic mechanical thermoanalysis or differential scanning calorimetry (DSC) studies.
  • DSC differential scanning calorimetry
  • the melting point can be determined using a standard melting point apparatus.
  • thermoplastic polymers 1. Thermoset or thermoplastic polymers.
  • the polymers can be thermoset or thermoplastic polymers, although thermoplastic polymers may be preferred due to their ease of molding.
  • the degree of crystallinity of the polymer or polymeric block(s) is between 3 and 80%, more preferably between 3 and 60%.
  • the degree of crystallinity is greater than 80% while all soft segments are amorphous, the resulting polymer composition has poor shape memory characteristics.
  • the tensile modulus of the polymers below the T tra ns is typically between 50 MPa and 2 GPa (gigapascals), whereas the tensile modulus of the polymers above the T ⁇ ans is typically between 1 and 500 MPa.
  • the ratio of elastic modulus above and below the T tra ns is 20 or more. The higher the ratio, the better the shape memory of the resulting polymer composition.
  • the polymer segments can be natural or synthetic, although synthetic polymers are preferred.
  • the polymer segments can be biodegradable or non- biodegradable, although the resulting SMP composition is biodegradable biocompatible polymers are particularly preferred for medical applications. In general, these materials degrade by hydrolysis, by exposure to water or enzymes under physiological conditions, by surface erosion, bulk erosion, or a combination thereof.
  • Non-biodegradable polymers used for medical applications preferably do not include aromatic groups, other than those present in naturally occurring amino acids.
  • Representative natural polymer segments or polymers include proteins such as zein, modified zein, casein, gelatin, gluten, serum albumin, and collagen, and polysaccharides such as alginate, celluloses, dextrans, pullulane, and polyhyaluronic acid, as well as chitin, poly(3- hydroxyalkanoate)s, especially poly( ⁇ -hydroxybutyrate), poly(3- hydroxyoctanoate) and poly(3-hydroxyfatty acids).
  • proteins such as zein, modified zein, casein, gelatin, gluten, serum albumin, and collagen
  • polysaccharides such as alginate, celluloses, dextrans, pullulane, and polyhyaluronic acid
  • chitin poly(3- hydroxyalkanoate)s, especially poly( ⁇ -hydroxybutyrate), poly(3- hydroxyoctanoate) and poly(3-hydroxyfatty acids).
  • Representative natural biodegradable polymer segments or polymers include polysaccharides such as alginate, dextran, cellulose, collagen, and chemical derivatives thereof (substitutions, additions of chemical groups, for example, alkyl, alkylene, hydroxylations, oxidations, and other modifications routinely made by those skilled in the art), and proteins such as albumin, zein and copolymers and blends thereof, alone or in combination with synthetic polymers.
  • Representative synthetic polymer blocks include polyphosphazenes, poly(vinyl alcohols), polyamides, polyester amides, poly(amino acid)s, synthetic poly(amino acids), polyanhydrides, polycarbonates, polyacrylates, polyalkylenes, polyacrylamides, polyalkylene glycols, polyalkylene oxides, polyalkylene terephthalates, polyortho esters, polyvinyl ethers, polyvinyl esters, polyvinyl halides, polyvinylpyrrolidone, polyesters, polylactides, polyglycolides, polysiloxanes, polyurethanes and copolymers thereof.
  • suitable polyacrylates include poly(methyl methacrylate), poly(ethyl methacrylate), poly(butyl methacrylate),
  • Synthetically modified natural polymers include cellulose derivatives such as alkyl celluloses, hydroxyalkyl celluloses, cellulose ethers, cellulose esters, nitrocelluloses, and chitosan.
  • Suitable cellulose derivatives include methyl cellulose, ethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, hydroxybutyl methyl cellulose, cellulose acetate, cellulose propionate, cellulose acetate butyrate, cellulose acetate phthalate, carboxymethyl cellulose, cellulose triacetate and cellulose sulfate sodium salt. These are collectively referred to herein as "celluloses".
  • Representative synthetic degradable polymer segments or polymers include polyhydroxy acids, such as polylactides, polyglycolides and copolymers thereof; poly(ethylene terephthalate); poly(hydroxybutyric acid); poly(hydroxyvaleric acid); poly[lactide-co-( ⁇ -caprolactone)]; poly[glycolide- co-( ⁇ -caprolactone)]; polycarbonates, poly(pseudo amino acids); poly(amino acids); poly(hydroxyalkanoate)s; polyanhydrides; polyortho esters; and blends and copolymers thereof.
  • polyhydroxy acids such as polylactides, polyglycolides and copolymers thereof
  • polycarbonates poly(pseudo amino acids); poly(
  • non-biodegradable polymer segments or polymers include ethylene vinyl acetate, poly(meth)acrylic acid, polyamides, polyethylene, polypropylene, polystyrene, polyvinyl chloride, polyvinylphenol, and copolymers and mixtures thereof.
  • Rapidly bioerodible polymers such as poly(lactide-co-glycolide)s, polyanhydrides, and polyorthoesters, which have carboxylic groups exposed on the external surface as the smooth surface of the polymer erodes, also can be used.
  • polymers containing labile bonds such as polyanhydrides and polyesters, are well known for their hydrolytic reactivity. Their hydrolytic degradation rates can generally be altered by simple changes in the polymer backbone and their sequence structure.
  • polymers such as polyacetylene and polypyrrole
  • conducting polymers are particularly preferred for uses in which electrical conductance is important. Examples of these uses include
  • tissue engineering and any biomedical application where cell growth is to be stimulated may find particular utility in the field of computer science, as they are able to absorb heat without increasing in temperature better than SMAs.
  • Conducting shape memory polymers are useful in the field of tissue engineering to stimulate the growth of tissue, for example, nerve tissue.
  • the polymer may be in the form of a hydrogel (typically absorbing up to about 90% by weight of water), and can optionally be ionically crosslinked with multivalent ions or polymers. Ionic crosslinking between soft segments can be used to hold a structure, which, when deformed, can be reformed by breaking the ionic crosslinks between the soft segments.
  • the polymer may also be in the form of a gel in solvents other than water or aqueous solutions. In these polymers, the temporary shape can be fixed by hydrophilic interactions between soft segments.
  • Hydrogels can be formed from polyethylene glycol, polyethylene oxide, polyvinyl alcohol, polyvinyl pyrrolidone, polyacrylates, poly (ethylene terephthalate), poly(vinyl acetate), and copolymers and blends thereof.
  • polymeric segments for example, acrylic acid, are elastomeric only when the polymer is hydrated and hydrogels are formed.
  • polymeric segments for example, methacrylic acid
  • polymeric block can be used, depending on the desired application and conditions of use.
  • shape memory is observed for acrylic acid copolymers only in the hydrogel state, because the acrylic acid units are substantially hydrated and behave like a soft elastomer with a very low glass transition temperature.
  • the dry polymers are not shape memory polymers. When dry, the acrylic acid units behave as a hard plastic even above the glass transition temperature and show no abrupt change in mechanical properties on heating. In contrast, copolymers including methyl acrylate polymeric segments as the soft segments show shape memory properties even when dry.
  • Certain polymers for example, poly(ethylene oxide-co-propylene oxide) (PLURONICSTM), are soluble in water at temperatures lower than body temperature and become hydrogels at temperatures higher than body temperature. Incorporation of these polymers as segments in shape memory polymers provides them with the ability to response to changes in temperature in a manner opposite that of typical shape memory polymers. These materials recover their shape when cooled below their shape recovery temperature, rather than being heated above their shape recovery temperature. This effect is called inversed thermal shape memory effect. Shape memory polymer compositions including these polymer segments are useful in various biomedical applications where the polymer can be inserted as a liquid, and cooled to recover an intended shape in situ. The inverse thermal shape memory effect can be obtained by incorporating two different segments into a polymer that are miscible at temperatures lower than T m i sc , but are immiscible at higher temperatures. The phase separation at higher temperatures stabilizes the temporary shape.
  • PLURONICSTM poly(ethylene oxide-co-propylene oxide)
  • the polymers can be obtained from commercial sources such as Sigma Chemical Co., St. Louis, MO.; Polysciences, Warrenton, PA; Aldrich Chemical Co., Milwaukee, WI; Fluka, Ronkonkoma, NY; and BioRad, Richmond, CA. Alternately, the polymers can be synthesized from monomers obtained from commercial sources, using standard techniques. II. Assembly of Polymer Segments
  • the shape memory polymer include one or more hard segments and one or more soft segments, wherein at least one of the segments is biodegradable or at least one of the segments is linked to another segment via a biodegradable linkage. Representative biodegradable linkages include ester-, amide-, anhydride-, carbonate-, or orthoester linkages.
  • the shape memory effect is based on the polymer morphology.
  • thermoplastic elastomers the original shape of an object is fixed by physical crosslinks caused by the hard segment.
  • thermoset polymers the soft segments are covalently crosslinked instead of having hard segments.
  • the original shape is set by the crosslinking process.
  • segmented polyurethane SMPs the segments of the compositions described herein need not be linear.
  • the segments can be partially grafted or attached in dendremeric side groups.
  • Thermoplastic and Thermoelastic Polymers can be in the form of linear diblock-, triblock-, tetrablock, or multiblock copolymers, branch or graft polymers, thermoplastic elastomers, which contain dendritic structures, and blends thereof.
  • Figure 3 illustrates some of the combinations of suitable classes of thermoplastic materials forming the hard and soft segments.
  • the thermoplastic shape memory polymer composition also can be a blend of one or more homo- or co-polymer with one or more diblock-, triblock-, tetrablock, or multiblock copolymers, branch or graft polymers. These types of polymers are well known to those of skill in the art.
  • thermoset refers to (i) thermosets SMPs containing only one soft segment, which contains cleavable bonds, and (ii) thermosets containing more than one soft segment, wherein at least one soft segment is degradable or wherein the different soft segments are connected by cleavable bonds.
  • thermoset polymers that have shape memory capability. These include polymer networks, semi-interpenetrating networks, interpenetrating networks, and mixed-interpenetrating networks.
  • a polymer network is prepared by covalently crosslinking macromonomers, i.e., polymers which contain polymerizable endgroups such as carbon-carbon double bonds.
  • the polymerization process can be induced by using light or heat sensitive initiators or by curing with ultraviolet light ("UN-light”) without an initiator.
  • Shape memory polymer networks are prepared by crosslinking one or more soft segments which correspond to one or more thermal transitions.
  • the crosslinking is performed using a photocrosslinker and requires no chemical
  • FIG. 14 is a diagram of a reaction sequence for the synthesis of a preferred photocrosslinker, which produces an overall yield of about 65%. //. Interpenetrating Networks
  • Interpenetrating networks are defined as networks where two components are crosslinked, but not to each other.
  • the original shape is determined by the network with the highest crosslink density and the highest mechanical strength.
  • the material has at least two Ttrans corresponding to the different soft segments of both networks.
  • Mixed Interpenetrating Network A mixed IPN includes at least one physically crosslinked polymer network (a thermoplastic polymer) and at least one covalently crosslinked polymer network (a thermoset polymer) that cannot be separated by any physical methods.
  • the original shape is set by the covalently crosslinked network.
  • the temporary shapes correspond to the Ttrans of the soft segments and the T tra ns of the hard segment of the thermoplastic elastomer component.
  • a particularly preferred mixed interpenetrating network is prepared by polymerizing a reactive macromonomer in the presence of a thermoplastic polymer, for example, by the photopolymerization of carbon-carbon double bonds.
  • the ratio by weight of thermoset polymer to thermoplastic polymer is preferably between 5:95 and 95:5, more preferably, between 20:80 and 80:20.
  • Semi-Interpenetrating Networks (“semi-IPN") are defined as two independent components, where one component is a crosslinked polymer (a polymer network) and the other component is a non-crosslinked polymer (a homopolymer or copolymer), wherein the components cannot be separated by physical methods.
  • the semi-IPN has at least one thermal transition corresponding to the soft segment(s) and the homo- or co-polymer components.
  • the crosslinked polymer preferably constitutes between about 10 and 90% by weight of the semi-interpenetrating network composition.
  • the shape memory polymer compositions described herein are formed of a biodegradable polymer blend.
  • a biodegradable polymer blend is a blend having at least one biodegradable polymer.
  • the shape memory polymers can exist as physical mixtures of thermoplastic polymers.
  • a shape memory polymer composition can be prepared by interacting or blending two thermoplastic polymers.
  • the polymers can be semicrystalline homopolymers, semicrystalline copolymers, thermoplastic elastomers with linear chains, thermoplastic elastomers with side chains or any kind of dendritic structural elements, and branched copolymers, and these can be blended in any combination thereof.
  • a multiblock copolymer with a hard segment with a relatively high T tra ns and a soft segment with a relatively low Tt ran s can be mixed or blended with a second multiblock copolymer with a hard segment with a relatively low T tra ns and the same soft segment as that in the first multiblock copolymer.
  • the soft segments in both multiblock copolymers are identical, so the polymers are miscible in each other when the soft segments are melted.
  • the mechanical properties of these polymers can be adjusted by the changing the weight ratio of the two polymers.
  • Other kinds of blends of at least two multiblock copolymers, in which at least one of the segments is miscible with at least one of the segments of the other multiblock copolymers, can be prepared. If two different segments are miscible and build one domain together, then the thermal transition of this domain depends on the weight content of the two segments. The maximum number of memorized shapes results from the number of thermal transitions of the blend.
  • Shape memory blends may have better shape memory capabilities than the blend components alone.
  • Shape memory blends are composed of at least
  • 16 least one multiblock copolymer and at least one homo- or copolymer.
  • di-, tri, tetra-block copolymers can be used instead of a multiblock copolymer.
  • Shape memory blends are highly useful in industrial applications, since a broad range of mechanical, thermal, and shape memory capabilities can be obtained from only two or three basic polymers by blending them in different weight ratios.
  • a twin screw extruder is an example of standard process equipment that could be used to mix the components and process the blend. m.
  • compositions can be formed into a first shape under appropriate conditions, for example, at a temperature above the T ran s of the hard segments, and allowed to cool below the Tt ra ns of the soft segment(s). Standard techniques are extrusion and injection molding.
  • the object can be re-formed into a second shape. Upon application of heat or other appropriate set of conditions, the object returns to original shape.
  • Thermoset polymers can be prepared by extruding the pre- polymerized material (macromonomers), and fixing the original shape at a temperature above the T ⁇ - of the thermoset polymer, for example, by photocuring reactive groups on the monomer.
  • the temporary shape is fixed by cooling the material below Ttr ans after deforming the material.
  • Figure 5 illustrates a photoinduced shape memory effect.
  • the crosslinking also can be performed in a solution of the macromonomers.
  • the solvent is removed from the formed gel in a subsequent step.
  • compositions formed of thermoplastic polymers can be blown, extruded into sheets or shaped by injection molding, for example, to form fibers.
  • the compositions can also be shaped by other methods known to
  • any of a variety of therapeutic, prophylactic and/or diagnostic agents can be incorporated within the polymer compositions, which can locally or systemically deliver the incorporated agents following administration to a patient.
  • Therapeutic. Diagnostic and Prophylactic Applications can be incorporated within the polymer compositions, which can locally or systemically deliver the incorporated agents following administration to a patient.
  • any of a variety of therapeutic agents can be incorporated within the particles, for local or systemic delivery of the incorporated agents following administration to a patient.
  • examples include synthetic inorganic and organic compounds or molecules, proteins and peptides, polysaccharides and other sugars, lipids, and nucleic acid molecules having therapeutic, prophylactic or diagnostic activities.
  • Nucleic acid molecules include genes, plasmid DNA, naked DNA, antisense molecules which bind to complementary DNA to inhibit transcription, ribozymes and ribozyme guide sequences.
  • the agents to be incorporated can have a variety of biological activities, such as vasoactive agents, neuroactive agents, hormones, growth factors, cytokines, anaesthetics, steroids, anticoagulants, anti-inflammatories, immunomodulating agents, cytotoxic agents, prophylactic agents, antibiotics, antivirals, antisense, antigens, and antibodies.
  • the proteins may be antibodies or antigens which otherwise would have to be administered by injection to elicit an appropriate response. Proteins are defined as consisting of 100 amino acid residues or more; peptides are less than 100 amino acid residues. Unless otherwise stated, the term protein refers to both proteins and peptides. Polysaccharides, such as heparin, can also be administered.
  • Imaging agents which may be utilized include commercially available agents used in positron emission tomography (PET), computer assisted tomography (CAT), single photon emission computerized
  • the SMP compositions can be used to prepare numerous articles of manufacture, for use in biomedical and other applications.
  • the polymer compositions can be used to prepare articles of manufacture for use in biomedical applications. For example, sutures, orthodontic materials, bone screws, nails, plates, catheters, tubes, films, stents, orthopedic braces, splints, tape for preparing casts, and scaffolds for tissue engineering, contact lenses, drug delivery devices, implants, and thermal indicators, can be prepared.
  • the SMP compositions are preferably prepared from biocompatible polymers, and, for most applications, from biodegradable polymers.
  • Biodegradable polymers degrade at a controlled rate depending on the composition and crosslinking of the polymer.
  • Degradable polymeric implants eliminate the need for implant retrieval and can be used simultaneously to deliver therapeutic agents.
  • the materials can be used in many applications requiring load- bearing capacities and controlled degradation.
  • the polymer compositions can be formed into the shape of an implant which can be implanted within the body to serve a mechanical function.
  • implants include rods, pins, screws, plates and anatomical shapes.
  • a particularly preferred use of the compositions is to prepare sutures that have a rigid enough composition to provide for ease of insertion, but upon attaining body temperature, soften and form a second shape that is more comfortable for the patient while still allowing healing.
  • a catheter can be rigid at body temperature for ease of insertion, but, after warming to body temperature, can soften to provide comfort to the patient.
  • the polymer compositions can be combined with fillers, reinforcement materials, radioimaging materials, excipients or other
  • fillers include calcium-sodium-metaphosphate which is described in U.S. Patent No. 5, 108,755. Those of skill in the art can readily determine a suitable amount of these materials to include in the compositions.
  • the articles can incorporate various therapeutic and/or diagnostic agents, as described above.
  • shape memory polymer compositions other than biomedical applications.
  • non-medical type applications for biodegradable polymers include items for which disposal is an issue, such as disposable diapers and packaging materials.
  • Shape memory polymers can be designed so that the degradation rate is varied.
  • a hydrolytically degradable polymer can be selectively protected by applying a hydrophobic SMP coating that temporarily prevents water from reaching the hydrolytically cleavable bonds of the bulk polymer.
  • the protective feature of the coating then can be modified when desired by applying an external stimulus such that the diffusion properties of coating are altered to permit water or other aqueous solutions to permeate through the coating and initiate the degradation process. If the hydrolysis rate is relatively high compared to the diffusion rate of water, then the diffusion rate of water through the coating determines the degradation rate.
  • a hydrophobic coating consisting of densely crosslinked soft segments can be used as a diffusion barrier for water or aqueous solutions. The soft segments should be at least partially crosslinked by linkages that can be cleaved by application of a stimulus. The diffusion rate of water can increased by lowering the crosslinking density. V ⁇ .
  • first shape is intended for an initial use
  • second shape is intended for a subsequent use.
  • biomedical devices which can form a second shape upon reaching at body temperature, or upon application of an external stimulus which heats the device above body temperature.
  • Still other articles of manufacture are designed to be used such that their shape changes in reaction to, or adjustment to, changes in temperature, such as thermosensers in medical devices.
  • Example 1 Copolyesterurethane Shape Memory Polymers A group of biocompatible and biodegradable multiblock-copolymers showing a thermal shape memory effect was synthesized. These polymers were composed of a crystallizable hard segment (T m ) and a soft segment having a thermal transition temperature T tra ns between room and body temperature. In contrast to the prior art segmented polyurethanes, the hard segment was an oligoester or an oligoetherester and did not contain any aromatic component.
  • the mechanism for programming the temporary shape and recovering the permanent shape of a multiblock-copolymer is shown in Figure 6.
  • the permanent shape of the materials was set by melting the polymer and cooling above Ttrans (Fig. 6 - top pos.). Then, the polymer was formed into its temporary shape (Fig. 6 - right pos.), which was fixed by cooling below Trans (Fig. 6 - bottom pos.). After unloading, the permanent shape was recovered by reheating above T trans .
  • the telechelic macrodiol were synthesized by ring opening polymerization of cyclic monomers with di(n-butyl)tinoxide as a transesterfication catalyst under a N 2 atmosphere. Hard Sesment
  • the product was soluted in hot 1,2-dichloroethane and filtered hot through a Buechner-funnel filled with silica gel.
  • the product was obtained by precipitation in hexanes and dried in vacuo for 6 h.
  • Poly( ⁇ -caprolactone)-diols with different M n are commercially available, for example, from Aldrich and Polysciences. PCL-2000 was used herein.
  • Amorphous ⁇ , ⁇ -dihydroxy [oligo(Z,-lactate-co-glycolate) ethylene oligo (L- lactate-c ⁇ -glycolate)] - (abbr.: PLGA2000-15) was prepared as follows. In a 1000 ml two-neck round bottomed flask, 300 g (2.08 mol) of L,L-dilactide, 45 g (034 mol) of diglycolide and 4.94 g (0.80 mol) ethylene glycol were heated to melt at 40 °C and stirred. 0.614 g (2.5 mmol) di(n-butyl) tinoxide was added.
  • Multiblock copolymers were prepared from the following two types 15 of polymers.
  • PDC polymers contain poly( ⁇ -caprolactone). T tra ns for the soft segment is the melting point.
  • PDL polymers contain a ⁇ , ⁇ -dihydroxy [oligo(Z.-lactate-co- glycolate) ethylene oligo ( -lactate-co-glycolate)].
  • Ttrans for the soft segment 20 is the glass transition point.
  • Ta ble 2 Synt hesis of M ultiblock Copolymers
  • the toxicity of two different multiblock-copolymers was investigated using a chicken egg test. It was shown that blood vessels developed regularly and their condition was not influenced by the polymer samples.
  • Ta ble 7 PDL22 Degradability
  • Figure 7 shows the results of tensile tests performed on the multiblock copolymers, as a function of the number of thermolytic cycles.
  • the average shape fixity rate of thermocyclicly treated polymers and the dependency of strain recovery rates as a function of the number of cycles is
  • the polymers have a high shape fixity, and an equilibrium state was achieved after only two cycles.
  • thermosets A range of poly( ⁇ -caprolactone) dimethacrylates and thermosets were evaluated for their mechanical and shape memory properties.
  • PCLDMAs Poly( ⁇ -caprolactone) dimethacrylates
  • the solution was stirred at 0 °C for 3 days and precipitated salt filtered off.
  • the macromonomer (or the monomer mixture) was heated to 10 °C above its melting temperature (T m ) and filled into a mould formed by two
  • Table 12 lists the poly( ⁇ -caprolactone) dimethacrylates that were prepared, along with the respective degree of acrylation (D a ) (%) The number following PCLDMA is the molecular weight M n of the poly( ⁇ - caprolactone) diol used in the synthesis as determined using ⁇ -NMR and GPC, rounded to 500.
  • Table 12 Poly( ⁇ -caprolactone) Diol and Degree of Acrylation
  • PCLDMA7000 PCLDMA10000 86
  • Figure 8 shows the melting temperature (T m ) of diols, dimethacrylates, and thermosets of poly( ⁇ -caprolactone) as a function of the molar mass weight M n of the macromonomers.
  • T m melting temperature
  • macrodiols are represented by - - ⁇ - - ; macromoners by ••• • •••• ; and thermosets by — — .
  • thermosets were determined to have the thermomechanical properties indicated in Table 15.
  • the number average molecular weights (M n ) is of the macromonomer.
  • the lower limit temperature, Ti is 0 °C, and the higher limit temperature, Th, is 70 °C.
  • R r (2) is the strain recovery rate of the second cycle
  • R r , to t is the total strain recovery rate after 5 cycles
  • R f is the average strain fixity rate.
  • Table 15 Thermoset Thermomechanical Properties name M n R (2) R-r,tot Rf [g-mol- 1 ] [%] [%] [%1

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RU2215542C2 (ru) 2003-11-10
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ATE266434T1 (de) 2004-05-15
DE69917224D1 (de) 2004-06-17
HUP0100466A3 (en) 2002-03-28
AU751861B2 (en) 2002-08-29
KR20010034275A (ko) 2001-04-25
JP2002503524A (ja) 2002-02-05
IL137299A0 (en) 2001-07-24
EP1056487B1 (de) 2004-05-12
DE69917224T2 (de) 2004-09-09
CA2316190C (en) 2005-09-13
WO1999042147A1 (en) 1999-08-26
KR100382568B1 (ko) 2003-05-09
CA2316190A1 (en) 1999-08-26
ES2221363T3 (es) 2004-12-16
CZ303404B6 (cs) 2012-08-29
IL137299A (en) 2007-06-03
AU2784599A (en) 1999-09-06
JP4034036B2 (ja) 2008-01-16
JP2007314797A (ja) 2007-12-06
CZ20003072A3 (en) 2001-06-13
TR200002450T2 (tr) 2001-01-22
HUP0100466A2 (hu) 2001-06-28
US6160084A (en) 2000-12-12
BR9907968B1 (pt) 2009-12-01
HU222543B1 (hu) 2003-08-28

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